D68.2

Hereditary deficiency of other clotting factors

Parent Code: D68

Inclusion Terms

  • • AC globulin deficiency
  • • Congenital afibrinogenemia
  • • Deficiency of factor I [fibrinogen]
  • • Deficiency of factor II [prothrombin]
  • • Deficiency of factor V [labile]
  • • Deficiency of factor VII [stable]
  • • Deficiency of factor X [Stuart-Prower]
  • • Deficiency of factor XII [Hageman]
  • • Deficiency of factor XIII [fibrin stabilizing]
  • • Dysfibrinogenemia (congenital)
  • • Hypoproconvertinemia
  • • Owren's disease
  • • Proaccelerin deficiency

Code First

None code first specified for this code.

Use Additional Code

None use additional code specified for this code.

Cannot Code Together

These codes cannot be used together with the current code, even if both conditions are present.

None specified for this code.

Can Code Together

These codes can be used together with the current code if both conditions are documented.

None specified for this code.